On the public citation graph

Allopolyploid origin of the leafy liverwort Plagiochila britannica (Plagiochilaceae)

https://doi.org/10.1093/botlinnean/bow005

0 signed · 79 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/tax.606006openalex-snapshot

Phylogeny, taxon circumscriptions, and character evolution in the core Ptychanthoideae (Lejeuneaceae, Marchantiophyta)

inferredcites →https://doi.org/10.1007/bf00120221openalex-snapshot

The hybrid origin of the polyploid liverwort Pellia borealis

inferredcites →https://doi.org/10.1007/bf00985369openalex-snapshot

Isozyme evidence regarding the origins of three allopolyploid species ofPolytrichastrum (Polytrichaceae, Bryophyta)

inferredcites →https://doi.org/10.1007/bf00985667openalex-snapshot

The leafy liverwortPorella baueri (Porellaceae) is an allopolyploid

inferredcites →https://doi.org/10.1007/bf01087035openalex-snapshot

Chloroplast DNA-relationship in palaeoaustralLopidium concinnum (Hypopterygiaceae, Musci). An example of stenoevolution in mosses Studies in austral temperate rain forest bryophytes 2

inferredcites →https://doi.org/10.1007/s00239-002-2375-4openalex-snapshot

Organellar Inheritance in Liverworts: An Example of Pellia borealis

inferredcites →https://doi.org/10.1007/s00606-004-0221-4openalex-snapshot

Cryptic speciation in Herbertus (Herbertaceae, Jungermanniopsida): Range and morphology of Herbertus sendtneri inferred from nrITS sequences

inferredcites →https://doi.org/10.1007/s00606-006-0408-yopenalex-snapshot

Reinstatement of Lophocoleaceae (Jungermanniopsida) based on chloroplast gene rbcL data: exploring the importance of female involucres for the systematics of Jungermanniales

inferredcites →https://doi.org/10.1007/s00606-011-0565-5openalex-snapshot

Allopolyploid speciation of Calypogeia sphagnicola (Jungermanniopsida, Calypogeiaceae) based on isozyme and DNA markers

inferredcites →https://doi.org/10.1007/s10265-009-0291-zopenalex-snapshot

Why does biparental plastid inheritance revive in angiosperms?

inferredcites →https://doi.org/10.1007/s13127-015-0258-yopenalex-snapshot

A phylogeny of Lophocoleaceae-Plagiochilaceae-Brevianthaceae and a revised classification of Plagiochilaceae

inferredcites →https://doi.org/10.1016/j.ympev.2008.06.015openalex-snapshot

Low-copy nuclear DNA sequences reveal a predominance of allopolyploids in a New Zealand Asplenium fern complex

inferredcites →https://doi.org/10.1016/s0065-2296(08)60331-6openalex-snapshot

Cytogenetics, Biosystematics and Evolution in the Bryophyta

inferredcites →https://doi.org/10.1016/s1360-1385(97)01154-0openalex-snapshot

Polyploidy in angiosperms

inferredcites →https://doi.org/10.1038/ncomms6134openalex-snapshot

Extant diversity of bryophytes emerged from successive post-Mesozoic diversification bursts

inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot

jModelTest 2: more models, new heuristics and parallel computing

inferredcites →https://doi.org/10.1038/srep05974openalex-snapshot

Epiphytic leafy liverworts diversified in angiosperm-dominated forests

inferredcites →https://doi.org/10.1043/0363-6445-26.1.66openalex-snapshot

The Narrow Endemic Sphagnum troendelagicum is an Allopolyploid Derivative of the Widespread S. balticum and S. tenellum

inferredcites →https://doi.org/10.1055/s-2003-44716openalex-snapshot

Reinstatement of Chiastocaulon Carl (Plagiochilaceae), Based on Evidence from Nuclear Ribosomal ITS and Chloroplast Gene rps4 Sequences

inferredcites →https://doi.org/10.1073/pnas.1213498109openalex-snapshot

Hornwort pyrenoids, carbon-concentrating structures, evolved and were lost at least five times during the last 100 million years

inferredcites →https://doi.org/10.1073/pnas.85.15.5601openalex-snapshot

Allopolyploidy in bryophytes: Multiple origins of Plagiomnium medium

inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot

A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood

inferredcites →https://doi.org/10.1086/314199openalex-snapshot

Genetic Relationships between Haploid and TriploidTargionia(Targioniaceae, Hepaticae)

inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot

MrBayes 3: Bayesian phylogenetic inference under mixed models

inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot

jModelTest: Phylogenetic Model Averaging

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026160openalex-snapshot

Markov Chasin Monte Carlo Algorithms for the Bayesian Analysis of Phylogenetic Trees

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026370openalex-snapshot

Phylogenetic Analysis Under Reticulate Evolution

inferredcites →https://doi.org/10.1093/sysbio/45.4.524openalex-snapshot

Testing for Phylogenetic Conflict Among Molecular Data Sets in the Tribe Triticeae (Gramineae)

inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot

Creating the CIPRES Science Gateway for inference of large phylogenetic trees

inferredcites →https://doi.org/10.1111/bij.12586openalex-snapshot

Phylogenetic structure and biogeography of the Pacific Rim clade ofSphagnumsubgen.Subsecunda: haploid and allodiploid taxa

inferredcites →https://doi.org/10.1111/boj.12279openalex-snapshot

Lobule shape evolution inRadula(Jungermanniopsida): one rate fits all?

inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00335.xopenalex-snapshot

Recent and recurrent polyploidy in Tragopogon (Asteraceae): cytogenetic, genomic and genetic comparisons

inferredcites →https://doi.org/10.1111/j.1095-8312.2009.01319.xopenalex-snapshot

Phylogeographic analyses reveal distinct lineages of the liverworts Metzgeria furcata (L.) Dumort. and Metzgeria conjugata Lindb. (Metzgeriaceae) in Europe and North America

inferredcites →https://doi.org/10.1111/j.1095-8312.2009.01340.xopenalex-snapshot

Allopolyploidy and homoploid hybridization in the Sphagnum subsecundum complex (Sphagnaceae: Bryophyta)

inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04113.xopenalex-snapshot

Three‐genome mosses: complex double allopolyploid origins for triploid gametophytes in Sphagnum

inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01341.xopenalex-snapshot

Maternal transmission of cytoplasmic DNA in interspecific hybrids of peat mosses, Sphagnum (Bryophyta)

inferredcites →https://doi.org/10.1111/j.1438-8677.1998.tb00737.xopenalex-snapshot

Allopolyploidy in the Thalloid Liverwort Corsinia (Marchantiales)

inferredcites →https://doi.org/10.1111/jbi.12385openalex-snapshot

Direct long‐distance dispersal shapes a New World amphitropical disjunction in the dispersal‐limited dung moss Tetraplodon (Bryopsida: Splachnaceae)

inferredcites →https://doi.org/10.1111/jbi.12779openalex-snapshot

Multiple transoceanic dispersals and geographical structure in the pantropical leafy liverwort Ceratolejeunea (Lejeuneaceae, Porellales)

inferredcites →https://doi.org/10.1111/nph.13698openalex-snapshot

On the relative abundance of autopolyploids and allopolyploids

inferredcites →https://doi.org/10.1127/0029-5035/2004/0078-0147openalex-snapshot

Delimitation of some European species of Calypogeia Raddi (Jungermanniales, Hepaticae) based on cytological characters and multienzyme phenotype

inferredcites →https://doi.org/10.1139/b04-139openalex-snapshot

What do we know about hybridization among bryophytes in nature?

inferredcites →https://doi.org/10.1163/9789004285385openalex-snapshot

The Liverwort Flora of the British Isles

inferredcites →https://doi.org/10.11646/phytotaxa.49.1.2openalex-snapshot

Molecular phylogenetic data on reticulate evolution in the genus Barbilophozia Löske (Anastrophyllaceae, Marchantiophyta) and evidence of non-concerted evolution of rDNA in Barbilophozia rubescens allopolyploid

inferredcites →https://doi.org/10.1179/037366810x12578498136075openalex-snapshot

Molecular cytogenetic analyses of haploid and allopolyploidPelliaspecies

inferredcites →https://doi.org/10.1179/174328206x90459openalex-snapshot

Interploidal gene flow and introgression in bryophytes:Sphagnum girgensohnii×S. russowii, a case of spontaneous neotriploidy

inferredcites →https://doi.org/10.1179/jbr.1979.10.3.245openalex-snapshot

Plagiochila britannica, a new species in the British Isles

inferredcites →https://doi.org/10.1179/jbr.1986.14.1.43openalex-snapshot

Bryophyte phylogeny in terms of chromosome cytology

inferredcites →https://doi.org/10.1179/jbr.1997.19.4.835openalex-snapshot

Plagiochila britannicaPaton, new to Spain

inferredcites →https://doi.org/10.1179/jbr.2000.22.1.17openalex-snapshot

Studies onPlagiochilasect.Plagiochila(Hepaticae) in East and South Asia

inferredcites →https://doi.org/10.12705/632.16openalex-snapshot

Three species for the price of one within the moss Homalothecium sericeum s.l.

inferredcites →https://doi.org/10.12705/635.32openalex-snapshot

Low‐copy nuclear data confirm rampant allopolyploidy in the Cystopteridaceae (Polypodiales)

inferredcites →https://doi.org/10.12705/642.5openalex-snapshot

Integrative taxonomy of Lepidolejeunea (Jungermanniopsida: Porellales): Ocelli allow the recognition of two neglected species

inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot

BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT

inferredcites →https://doi.org/10.1508/cytologia.64.37openalex-snapshot

Changes in Plastid DNA Content during the Life Cycle of the Hornwort Anthoceros punctatus L.

inferredcites →https://doi.org/10.1515/biorc-2015-0022openalex-snapshot

Two ploidy levels of genetically delimited groups of the Calypogeia fissa complex (Jungermanniopsida, Calypogeiaceae)

inferredcites →https://doi.org/10.1639/0007-2745(1998)101[61:tdiriw]2.0.co;2openalex-snapshot

Taxa Delimitation in Reboulia Investigated with Morphological, Cytological, and Isozyme Markers

inferredcites →https://doi.org/10.1639/0007-2745(2000)103[0357:meorei]2.0.co;2openalex-snapshot

Molecular Evidence of Reticulate Evolution in the Peatmosses (Sphagnum), IncludingS. ehyalinum sp. nov.

inferredcites →https://doi.org/10.1639/0007-2745-116.3.229openalex-snapshot

Isozyme evidence regarding the nature of polyploidy in the moss genus Cinclidium (Mniaceae)

inferredcites →https://doi.org/10.1639/0007-2745-117.2.187openalex-snapshot

Invisible in plain sight: recurrent double allopolyploidy in the African Sphagnum ×planifolium (Sphagnaceae)

inferredcites →https://doi.org/10.2307/1221954openalex-snapshot

Introduction to Bryology

inferredcites →https://doi.org/10.2307/2419725openalex-snapshot

Isozyme Evidence of Reticulate Evolution in Mosses: Plagiomnium medium is an Allopolyploid of P. ellipticum x P. insigne

inferredcites →https://doi.org/10.2307/25065367openalex-snapshot

Organellar inheritance in the allopolyploid moss Rhizomnium pseudopunctatum

inferredcites →https://doi.org/10.3732/ajb.1100115openalex-snapshot

Formalizing morphologically cryptic biological entities: New insights from DNA taxonomy, hybridization, and biogeography in the leafy liverwort Porella platyphylla (Jungermanniopsida, Porellales)

inferredcites →https://doi.org/10.3732/ajb.1400190openalex-snapshot

Evidence for reciprocal origins in Polypodium hesperium (Polypodiaceae): A fern model system for investigating how multiple origins shape allopolyploid genomes

inferredcites →https://doi.org/10.3732/ajb.1400494openalex-snapshot

Hybridization is associated with changes in sexual system in the bryophyte genus Atrichum

inferredcites →https://doi.org/10.3897/phytokeys.27.5523openalex-snapshot

Integrative taxonomy resolves the cryptic and pseudo-cryptic Radula buccinifera complex (Porellales, Jungermanniopsida), including two reinstated and five new species

inferredcites →https://doi.org/10.3897/phytokeys.8.2496openalex-snapshot

Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.15298/arctoa.29.04zenodo-depositor-declared

Contribution to the liverwort flora of Franz Josef Land Archipelago I. Liverworts (Marchantiophyta) of Ziegler Island

inferred← citeshttps://doi.org/10.1002/brv.70127openalex-snapshot

Why are so few island bryophytes endemic?

inferred← citeshttps://doi.org/10.1016/j.ympev.2016.12.018openalex-snapshot

By how much do we underestimate species diversity of liverworts using morphological evidence? An example from Australasian Plagiochila (Plagiochilaceae: Jungermanniopsida)

inferred← citeshttps://doi.org/10.1080/0028825x.2017.1318756openalex-snapshot

The New Zealand endemic Plagiochila caducifolia is a disjunct population of Plagiochila spinulosa (Plagiochilaceae: Jungermanniopsida)

inferred← citeshttps://doi.org/10.1093/botlinnean/box041openalex-snapshot

The moss Helicophyllum torquatum (Bryopsida: Helicophyllaceae) has survived since at least the Miocene

inferred← citeshttps://doi.org/10.1093/botlinnean/boy068openalex-snapshot

Nuclear multi-locus phylogenetic inferences of polyploidIsoëtesspecies (Isoëtaceae) suggest several unknown diploid progenitors and a new polyploid species from South America

inferred← citeshttps://doi.org/10.1111/jse.12502openalex-snapshot

Maintenance of genetic and morphological identity in two siblingSyrrhopodonspecies (Calymperaceae, Bryopsida) despite extensive introgression

inferred← citeshttps://doi.org/10.1111/jse.13159openalex-snapshot

A deep dive into bryophyte genome space reveals opposing evolutionary trends in the sister lineages, mosses and liverworts

inferred← citeshttps://doi.org/10.11646/bde.43.1.14openalex-snapshot

Evidence for interspecific hybridization in bryophytes during pre-molecular and molecular eras

inferred← citeshttps://doi.org/10.15298/arctoa.34.04openalex-snapshot

Lophozia savicziae Schljakov (Lophoziaceae, Marchantiophyta) – one more allopolyploid species of liverworts

inferred← citeshttps://doi.org/10.7751/telopea12959openalex-snapshot

A revision of Australian Plagiochila (Lophocoleinae: Jungermanniopsida)

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.